ClinVar Miner

List of variants in gene combination LOC110121269, SCN5A reported as likely benign by GeneDx

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_000335.5(SCN5A):c.3229-33G>A rs41313657 0.00346
NM_000335.5(SCN5A):c.3228+6C>G rs368048551 0.00019
NM_000335.5(SCN5A):c.3207G>A (p.Thr1069=) rs371686822 0.00008
NM_000335.5(SCN5A):c.3047C>T (p.Thr1016Met) rs199473185 0.00006
NM_000335.5(SCN5A):c.3068G>A (p.Arg1023His) rs199473592 0.00006
NM_000335.5(SCN5A):c.3243G>A (p.Val1081=) rs41312407 0.00006
NM_000335.5(SCN5A):c.3336C>T (p.Ala1112=) rs373679015 0.00006
NM_000335.5(SCN5A):c.2957G>A (p.Arg986Gln) rs41313667 0.00005
NM_000335.5(SCN5A):c.3080G>A (p.Arg1027Gln) rs763891399 0.00004
NM_000335.5(SCN5A):c.3033G>C (p.Pro1011=) rs764425131 0.00003
NM_000335.5(SCN5A):c.3111C>A (p.Gly1037=) rs1057521031 0.00003
NM_000335.5(SCN5A):c.3156C>T (p.Ala1052=) rs748975536 0.00003
NM_000335.5(SCN5A):c.2931C>G (p.Thr977=) rs780713625 0.00002
NM_000335.5(SCN5A):c.2976C>T (p.Pro992=) rs193922725 0.00002
NM_000335.5(SCN5A):c.3132C>T (p.Pro1044=) rs547709944 0.00002
NM_000335.5(SCN5A):c.3316G>A (p.Glu1106Lys) rs199473193 0.00002
NM_000335.5(SCN5A):c.3192G>A (p.Glu1064=) rs886039126 0.00001
NM_000335.5(SCN5A):c.3258G>A (p.Glu1086=) rs727504924 0.00001
NM_000335.5(SCN5A):c.3273C>T (p.Ser1091=) rs1057520359 0.00001
NM_000335.5(SCN5A):c.2788-15C>G rs1057522116
NM_000335.5(SCN5A):c.2841C>T (p.Leu947=) rs2061580908
NM_000335.5(SCN5A):c.3033G>A (p.Pro1011=) rs764425131
NM_000335.5(SCN5A):c.3117C>T (p.Pro1039=) rs762151891
NM_000335.5(SCN5A):c.3159G>A (p.Glu1053=) rs775605367
NM_000335.5(SCN5A):c.3240T>C (p.Pro1080=) rs2125867954
NM_000335.5(SCN5A):c.3315C>T (p.Ala1105=) rs377603706

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